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Adrenal pheochromocytoma in a patient with Lynch Syndrome
Lynch Syndrome (LS), or hereditary non-polyposis colorectal cancer, is the most common cause of hereditary colorectal cancer. There are well described extra-colonic manifestations of LS, including gynecologic and upper urinary tract malignancies. Other extra-colonic manifestations of LS are less und...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073213/ https://www.ncbi.nlm.nih.gov/pubmed/35530545 http://dx.doi.org/10.1016/j.eucr.2022.102015 |
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author | Rodriguez, Katherine M. Harris, Kelly T. Singla, Nirmish |
author_facet | Rodriguez, Katherine M. Harris, Kelly T. Singla, Nirmish |
author_sort | Rodriguez, Katherine M. |
collection | PubMed |
description | Lynch Syndrome (LS), or hereditary non-polyposis colorectal cancer, is the most common cause of hereditary colorectal cancer. There are well described extra-colonic manifestations of LS, including gynecologic and upper urinary tract malignancies. Other extra-colonic manifestations of LS are less understood. Here we present an unusual case of a functional adrenal pheochromocytoma in a 31-year old man with LS. |
format | Online Article Text |
id | pubmed-9073213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90732132022-05-07 Adrenal pheochromocytoma in a patient with Lynch Syndrome Rodriguez, Katherine M. Harris, Kelly T. Singla, Nirmish Urol Case Rep Oncology Lynch Syndrome (LS), or hereditary non-polyposis colorectal cancer, is the most common cause of hereditary colorectal cancer. There are well described extra-colonic manifestations of LS, including gynecologic and upper urinary tract malignancies. Other extra-colonic manifestations of LS are less understood. Here we present an unusual case of a functional adrenal pheochromocytoma in a 31-year old man with LS. Elsevier 2022-02-03 /pmc/articles/PMC9073213/ /pubmed/35530545 http://dx.doi.org/10.1016/j.eucr.2022.102015 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Oncology Rodriguez, Katherine M. Harris, Kelly T. Singla, Nirmish Adrenal pheochromocytoma in a patient with Lynch Syndrome |
title | Adrenal pheochromocytoma in a patient with Lynch Syndrome |
title_full | Adrenal pheochromocytoma in a patient with Lynch Syndrome |
title_fullStr | Adrenal pheochromocytoma in a patient with Lynch Syndrome |
title_full_unstemmed | Adrenal pheochromocytoma in a patient with Lynch Syndrome |
title_short | Adrenal pheochromocytoma in a patient with Lynch Syndrome |
title_sort | adrenal pheochromocytoma in a patient with lynch syndrome |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073213/ https://www.ncbi.nlm.nih.gov/pubmed/35530545 http://dx.doi.org/10.1016/j.eucr.2022.102015 |
work_keys_str_mv | AT rodriguezkatherinem adrenalpheochromocytomainapatientwithlynchsyndrome AT harriskellyt adrenalpheochromocytomainapatientwithlynchsyndrome AT singlanirmish adrenalpheochromocytomainapatientwithlynchsyndrome |